Total synthesis of ribisin A
文献类型：期刊论文
| 作者 | Zhang, Chaoli ; Liu, Jun ; Du, Yuguo |
| 刊名 | TETRAHEDRON LETTERS
 |
| 出版日期 | 2014 |
| 卷号 | 55期号:4页码:959-961 |
| 关键词 | Ribisin A Benzofuran Total synthesis Ferrier carbocyclization Wacker oxidation |
| ISSN号 | 0040-4039 |
| 中文摘要 | The first total synthesis of natural product ribisin A has been achieved in 11 steps from commercially available methyl a-o-glucopyranoside with 21.6% overall yield. The highly oxygenated benzofuran skeleton of this natural product was constructed, taking advantages of the inherent chirality of o-glucose, through the key reactions of Ferrier carbocyclization, Johnson iodination, Suzuki cross-coupling, and Wacker oxidative cyclization. (C) 2013 Elsevier Ltd. All rights reserved. |
| WOS记录号 | WOS:000330604500043 |
| 公开日期 | 2015-03-24 |
| 源URL | [http://ir.rcees.ac.cn/handle/311016/9484]  |
| 专题 | 生态环境研究中心_环境化学与生态毒理学国家重点实验室 生态环境研究中心_中国科学院环境生物技术重点实验室 |
| 推荐引用方式 GB/T 7714 | Zhang, Chaoli,Liu, Jun,Du, Yuguo. Total synthesis of ribisin A[J]. TETRAHEDRON LETTERS,2014,55(4):959-961. |
| APA | Zhang, Chaoli,Liu, Jun,&Du, Yuguo.(2014).Total synthesis of ribisin A.TETRAHEDRON LETTERS,55(4),959-961. |
| MLA | Zhang, Chaoli,et al."Total synthesis of ribisin A".TETRAHEDRON LETTERS 55.4(2014):959-961. |
入库方式： OAI收割
来源：生态环境研究中心
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